Sodium Methoxide → 2-Methoxyoxazole-5-carboxylic acid
Reaction equation
Cl[C:2]1[O:3][C:4]([C:7]([O:9]CC)=[O:8])=[CH:5][N:6]=1.[CH3:12][O-:13].[Na+]>CC#N.CO>[CH3:12][O:13][C:2]1[O:3][C:4]([C:7]([OH:9])=[O:8])=[CH:5][N:6]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of ethyl 2-chlorooxazole-5-carboxylate (510 mg, 2.90 mmol) in anhdryous MeCN (10 mL) and anhydrous MeOH (10 mL) is added NaOMe (628 mg, 11.62 mmol). The crude is stirred at reflux for 2 hrs. To this crude is added additional MeOH. The crude is refluxed for another 4 hrs. The crude is concentrated and is redissolved in MeOH (10 mL). To this crude is added 1 N NaOH (10 ml). The crude is stirred at room temperature for 3 hrs. The crude is quenched with concentrated HCl, PH adjusted to 7 via PH paper indicator. The crude is concentrated and diluted in water. The aq. layer is acidified with concentrated HCl and diluted in EtOAc. The organic layer is washed with water, brine, dried over MgSO4, filtered, and concentrated to give 2-methoxyoxazole-5-carboxylic acid (290 mg). HPLC retention time=0.58 minutes (condition D); MS (m+1)=144.0.
Workup
- temperatureat reflux for 2 hrs
- temperatureThe crude is refluxed for another 4 hrs
- concentrationThe crude is concentrated
- dissolutionis redissolved in MeOH (10 mL)
- additionTo this crude is added 1 N NaOH (10 ml)
- stirringThe crude is stirred at room temperature for 3 hrs
- customThe crude is quenched with concentrated HCl, PH
- concentrationThe crude is concentrated
- additiondiluted in water
- additiondiluted in EtOAc
- washThe organic layer is washed with water, brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-bc15f505035b4ff9a9b9f2ae213a5384
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08822534B2
Reaction notes
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